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Ito et al., 2020 - Google Patents

Systematic Control of Structural and Photophysical Properties of π‐Extended Mono‐and Bis‐BODIPY Derivatives

Ito et al., 2020

Document ID
8118808706192763245
Author
Ito H
Sakai H
Suzuki Y
Kawamata J
Hasobe T
Publication year
Publication venue
Chemistry–A European Journal

External Links

Snippet

A series of π‐extended mono‐and bis‐BODIPY (BODIPY= boron‐dipyrromethene) derivatives, namely, benzo [a] phenanthrene‐fused BODIPY (Phena‐Mono‐BDP), benzo [a] anthracene‐fused BODIPY (Ant‐Mono‐BDP), and dibenz [a, h] anthracene (DBA)‐bridged …
Continue reading at chemistry-europe.onlinelibrary.wiley.com (other versions)

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    • H—ELECTRICITY
    • H01—BASIC ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
    • H01L51/0062—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
    • H01L51/0071—Polycyclic condensed heteroaromatic hydrocarbons
    • H01L51/0072—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ringsystem, e.g. phenanthroline, carbazole
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    • H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
    • H01L51/0052—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
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    • H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0077—Coordination compounds, e.g. porphyrin
    • H01L51/0079—Metal complexes comprising a IIIB-metal (B, Al, Ga, In or TI), e.g. Tris (8-hydroxyquinoline) gallium (Gaq3)
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    • H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0077—Coordination compounds, e.g. porphyrin
    • H01L51/0084—Transition metal complexes, e.g. Ru(II)polypyridine complexes
    • H01L51/0085—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising Iridium
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    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
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    • C09K2211/1018—Heterocyclic compounds
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